Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_assertion wasGeneratedBy ECO_0000203 NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_assertion wasDerivedFrom befree-20140225 NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_assertion SIO_000772 19407509 NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_assertion evidence source_evidence_literature NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_assertion description "[The rarity of MEN1 mutations in some MEN1-like states aids the identification of other mutated genes, such as AIP, HRPT2 and p27(Kip1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP319597.RAf5Eo1vxfVTDr9bj2FxfuUPgESNydj8n5Hw-P1CdXBPA130_provenance.